1-Boc-4-(chloromethyl)piperidine
97%
- Product Code: 173016
CAS:
479057-79-9
| Molecular Weight: | 233.74 g./mol | Molecular Formula: | C₁₁H₂₀ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08689676 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of active pharmaceutical ingredients (APIs) involving piperidine derivatives. Its Boc-protected amine group allows for selective reactivity, making it valuable in multi-step organic syntheses where controlled deprotection and functionalization are required. The chloromethyl group serves as a reactive handle for nucleophilic substitution, enabling the introduction of various side chains or heterocyclic systems. Commonly employed in the preparation of central nervous system agents, including analgesics, antipsychotics, and other bioactive molecules. Also utilized in medicinal chemistry for library synthesis in drug discovery due to its structural versatility and compatibility with solid-phase and solution-phase peptide-like synthesis techniques.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,310.00 |
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| 1g | 10-20 days | ฿3,560.00 |
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| 5g | 10-20 days | ฿16,500.00 |
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1-Boc-4-(chloromethyl)piperidine
Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of active pharmaceutical ingredients (APIs) involving piperidine derivatives. Its Boc-protected amine group allows for selective reactivity, making it valuable in multi-step organic syntheses where controlled deprotection and functionalization are required. The chloromethyl group serves as a reactive handle for nucleophilic substitution, enabling the introduction of various side chains or heterocyclic systems. Commonly employed in the preparation of central nervous system agents, including analgesics, antipsychotics, and other bioactive molecules. Also utilized in medicinal chemistry for library synthesis in drug discovery due to its structural versatility and compatibility with solid-phase and solution-phase peptide-like synthesis techniques.
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